Clinical Research Coordinator Job at Clear Dermatology & Aesthetics Center, Scottsdale, AZ

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  • Clear Dermatology & Aesthetics Center
  • Scottsdale, AZ

Job Description

The Clinical Research Coordinator is responsible for the coordination and administration of clinical trials under the direction and supervision of the Principal Investigator.

● Carry out clinical trial activities by adhering to Good Clinical Practice and study protocols

● Maintain the integrity of data while protecting the rights, safety, and well-being of patients enrolled in clinical trials

● Perform phlebotomy, EKGs, and obtain vital signs

● Work closely with study monitors to coordinate and carry out Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits, and Close-Out Visits.

● Complete Feasibility Questionnaires with PI and reach out to pharmaceutical and device companies to participate in new studies

● Communicate with Institutional Review Boards to maintain the proper oversight of clinical trials

● Day-to-day oversight of the research team

● Ensure research staff remains on task throughout the work day

○ Maintain a professional environment

○ Delegation and prioritization of tasks

● Oversee recruitment of research studies in collaboration with the protocol specific CRCs and research assistants to ensure referrals are contacted within 24-hours and recruitment portals are maintained up-to-date

● Manage batch shipment schedule Monday-Thursday based off of clinic and staff schedules

● Work with protocol specific CRCs to ensure that binders are kept audit ready at all times

● Ensure temperature controlled areas are maintained at the proper temperature and that temperature readings are documented daily upon arrival to the site

● Ensure that Calibration Log is kept up-to-date

● Ensure that research staff is following Research Task List in downtime

● Manage the research calendar in accordance with Investigator schedules

● Work with protocol specific lead CRCs to ensure that data entry and queries are attended to within a timely manner and per Clinical Trial Agreement timelines

● Confirm that staff training is up-to-date at all times. Work with protocol specific CRCs to ensure that delegated staff trainings are up-to-date

**Please submit cover letter to be considered for this position.

Job Tags

Interim role,

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